HYDROBRUSH (TM) KERATOME— 510(k) K971078
Substantially EquivalentMedjet, Inc.
FDA 510(k) clearance K971078 for HYDROBRUSH (TM) KERATOME, Substantially Equivalent on 1998-01-23. Applicant: Medjet, Inc.. Device class: 1.
Clearance details
- Applicant
- Medjet, Inc.
- Product code
- Code HQS
- Device class
- Class 1
- Regulation
- 21 CFR 886.4070
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Edison, NJ, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.